Product safety of any PEMF system is the most basic and critical requirement. Proof of safety is defined by international regulations and the following norms have to be fulfilled by a PEMF manufacturer in order to legally market the device:
A) Electrical safety: Provision of a valid “CE” Certificate (electrical safety and electromagnetic compatibility), in the USA it can be also labelled as “UL”, in Canada as “CSA”!
B) Every PEMF manufacturer/supplier, advertising health/medical claims, needs to label their product with the official “CE” mark, followed by four digits, i.e. CE 0123 (the four digits representing the notified body to certify the device for the manufacturer/supplier) The four digits also validate the listing and approval of the country where the device is being marketed! In other words, the labeling assures that the respective product is legally registered and certified as an audited medical device, considered to be safe to use!
